BACKGROUND OF THE INVENTION
1. Field of the Invention
[0001] The invention relates generally to a process for reducing the particle size of solid
biomass material, and to compositions obtained by the process. The compositions comprise
solid biomass coated onto solid catalyst particles.
2. Description of the Related Art
[0002] PCT-EP2007-057269 describes a process whereby biomass and inorganic particulate materials are contacted
in such a way, for example by agitation with a gas, that the particle size of the
biomass is reduced. One of the downsides of this process that catalyst fines become
mixed with biomass ash in subsequent processing. The catalyst fines are difficult
to separate from the ash, resulting in a loss of catalyst material. Another disadvantage
of the earlier method is that biomass particles smaller than about 500 micrometers
may become separated from the reaction mixture and escape conversion.
[0003] In addition, it is desirable to use attrition-resistant catalyst particles in catalytic
cracking processes, so as to maintain the desired catalyst particle size as much as
possible during the process.
[0004] In addition, it is desirable to be able to separate biomass fines such as the inorganic
ash from the catalyst particles. If the catalyst particles are larger than the fines
this can be easily done by the well known particle separation methods.
[0005] Thus, there is a particular need for a process for reducing the particle size of
a solid biomass material and for providing intimate contact with a particulate solid
catalyst material. There is a further need for providing a process that avoids the
formation of catalyst fines, and allows for the capture of biomass fines.
[0006] There is a further need for biomass material in a form that allows it to be included
in the feed of a refinery process, such as fluid catalytic cracking (FCC), hydroprocessing,
thermal conversion, coking, reforming, steam reforming, and the like, while minimizing
or avoiding problems typically associated with the presence of solid particles in
the feed, such as catalyst plugging and pressure drop build-up.
BRIEF SUMMARY OF THE INVENTION
[0007] The present invention addresses these problems by providing a process for reducing
the particle size of a biomass material, said process comprising the steps of:
a) providing a biomass material;
b) reducing the particle size of the biomass material c) mixing the biomass material
of step b) with a fluidizable inorganic particulate material
d) subjecting the mixture of step c) to a gas stream, whereby the particle size of
the biomass material is reduced further.
[0008] Another aspect of the invention comprises a composition of matter comprising solid
biomass material coated onto a particulate solid catalyst material.
[0009] Yet another aspect of the invention comprises subjecting the biomass-coated particulate
catalyst material to a conversion process, such as a fluid catalytic cracking process.
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
[0010] The following is a description of certain embodiments of the invention, given by
way of example only.
[0011] In one embodiment the invention is a process for reducing the particle size of a
biomass material, said process comprising the steps of:
- a) providing a biomass material;
- b) reducing the particle size of the biomass material to a particle size range preferably
suitable for fluidization of the biomass material;
- c) mixing the biomass material of step b) with a fluidizable inorganic particulate
material;
- d) subjecting the mixture of step c) to fluidization conditions, whereby the particle
size of the biomass material is reduced further.
[0012] The biomass material of step a) may be any suitable biomass material. Examples include
biomass of aquatic origin, specifically biomass material derived from algae, and biomass
derived from land-based plants. The latter type generally contains ligno-cellulosic
material. It is desirable to use agricultural or forestry waste products as a source
of biomass material. Examples include straw, corn husks, bagasse, wood chips, saw
dust, and the like.
[0013] The purpose of step b) is to convert the solid biomass to a particle size range preferably
suitable for fluidization conditions. As the density of biomass is much less than
that of the inorganic particulate material, fluidizable biomass particles in general
have a larger particle diameter. In general, biomass material is fluidizable under
normal conditions if it has a particle size in the range of from 0.5 mm to about 0.05
mm. Suitable processes for obtaining such particle sizes include abrasion, shredding,
grinding, milling, and kneading.
[0014] In step c), the preferably fluidizable solid biomass material is mixed with a fluidizable
particulate inorganic material. The particulate inorganic material generally has a
mean particle size in the range of from 10 to 1000 microns. The particulate inorganic
material may be inert, or it may have catalytic properties. For the purpose of the
present invention a particulate inorganic material is considered as having catalytic
properties if it catalyzes the subsequent conversion of the solid biomass to bio-oil,
as explained herein below. A particulate inorganic material is considered as being
inert if it does not substantially catalyze this subsequent conversion. Sand (SiO
2) is an example of an inert particulate inorganic material.
[0015] It is preferred to employ particulate inorganic materials having catalytic properties.
Examples include zeolites, clays, hydrotalcites and hydrotalcite-like materials, refractory
oxides such as alumina, silica-alumina, zirconia, earth alkaline alkali metal hydroxides
and salts, in particular CaO, K
2CO
3, and the like. The catalytic properties of these materials may be modified by well-known
techniques, such as adding additives, depositing metals or metal oxides, modifying
the pore size distribution and/or pore volume, and the like.
[0016] In a specific embodiment the catalytic material comprises an alkali metal carbonate
and an inorganic base, such as the hydroxide of an earth alkaline metal (Ca, Mg) or
of aluminum.
[0017] Particularly desirable inorganic materials include used sand-blasting grit, and used
catalyst materials from other processes (such as E-cat from a refinery's FCC process),
because these materials are available at low cost, and have considerable catalytic
properties. In the case of used sand-blasting grit the catalytic properties stem from
metals that have become mixed with the grit during its use in sand-blasting.
[0018] Other desirable inorganic materials are Inorganic Carbonates, such as Sodium Carbonate,
Potassium Carbonate, Calcium Carbonate, Magnesium Carbonate and the like.
[0019] It may be desirable to increase the attrition resistance of the particulate inorganic
material. Techniques for increasing the attrition resistance of particulate inorganic
materials are well known in the art, in particular in the field of fluid catalytic
cracking (FCC).
[0020] Any suitable technique may be used for mixing the fluidizable solid biomass particles
with the fluidizable inorganic particulate material. However, the preferred method
comprises feeding gas-borne streams of both types of particles into a fluidized bed
reactor, such as an FCC riser. In general, the solid particulate biomass and the inorganic
particulate material are mixed in a weight ratio in the range of from 1:50 to 50:1.
[0021] The mixture obtained in step c) is subjected to abrasion via fluidization, fast fluidization
and/or solids flow conditions. The fluidizing gas may be air or some other oxygen-containing
gas. Preferably, however, the fluidizing gas is oxygen-poor or substantially oxygen-free.
During this fluidization step the impact of particles of the inorganic material colliding
with the biomass material results in a further reduction of the particle size of the
biomass material. Initially the inorganic particles are smaller than the biomass particles,
and inorganic particles may tend to become embedded in the biomass particles, as described
in
PCT-EP2007-057269. As the abrasion step continues, the biomass particles become smaller. The inorganic
particles, however, being much harder than the biomass particles, substantially maintain
their size.
[0022] The process of step d) is preferably carried out at ambient temperature, or a slightly
increased temperature.
[0023] With time, the inorganic particles become coated with biomass material. As used herein,
the terms "coated" and "coated onto" refer to inorganic particles having biomass material
at least at their outer surface, optionally also within their pores, if the inorganic
material is porous. The coating can be observed by techniques such as optical microscopy,
electron microscopy, TEM, SEM, and the like.
[0024] In another aspect, this invention relates to inorganic particulate materials coated
with solid biomass material, as obtained, for example, by the above-described process.
The particles are particularly suitable for use in a conversion process for converting
biomass to, for example, bio-oil. Preferably the conversion process uses a fluidized
bed, as the particles have the appropriate size for fluidization.
[0025] The subsequent conversion process may be carried out ion conventional refinery equipment,
such as a fluid catalytic cracker, a thermal cracker, a coker, a flexi coker an ebullated
bed conversion unit such as a hydrotreater, hydrocracker, an H-Oil unit and/or LC-finer,
fixed bed hydro conversion units and the like.
[0026] Thus, the invention has been described by reference to certain embodiments discussed
above. It will be recognized that these embodiments are susceptible to various modifications
and alternative forms well known to those of skill in the art.. Accordingly, although
specific embodiments have been described, these are examples only and are not limiting
upon the scope of the invention.
1. A process for reducing the particle size of a biomass material, said process comprising
the steps of:
a) providing a biomass material;
b) reducing the particle size of the biomass material
c) mixing the biomass material of step b) with a fluidizable inorganic particulate
material;
d) subjecting the mixture of step c) to fluidization and/or flow conditions, whereby
the particle size of the biomass material is reduced further.
2. The process of claim 1 wherein the particle size of the biomass material obtained
in step b) is in the range of 50 to 5000 microns.
3. The process of claim 1 wherein the fluidizable inorganic particulate material has
a particle size in the range of from 10 to 200 microns.
4. The process of claim 1 wherein the biomass material is of aquatic origin
5. The process of any one of the preceding claims wherein the biomass material is a lignocellulosic
biomass material.
6. The process of any one of the preceding claims wherein the biomass material is a mixture
of biomass solids and biomass liquids.
7. The process of any one of the preceding claims wherein the biomass material contains
and/or is mixed with municipal waste containing natural and synthetic polymers.
8. The process of any one of the preceding claims wherein the biomass material of step
a) has a moisture content of less than 50 wt%.
9. The process of any one of the preceding claims wherein the biomass material of step
a) has a moisture content of less than 10 wt%.
10. The process of any one of the preceding claims wherein the inorganic particulate material
comprises a catalytic material.
11. The process of claim 6 wherein the catalytic material is selected from the group consisting
of zeolites, clays, hydrotalcites and hydrotalcite-like materials, refractory oxides
such as alumina, silica-alumina, zirconia, earth alkaline alkali metal hydroxides
and salts and mixtures thereof.
12. The process of claim 6 wherein the catalytic material comprises an alkali metal carbonate
and a hydroxide of an earth alkaline metal or aluminum.
13. The process of any one of the preceding claims wherein the mixture of step c) has
a weight ratio biomass material : inorganic particulate material of from 1:50 to 50:1.
14. The process of any one of the preceding claims wherein the mixture of step c) has
a weight ratio biomass material : inorganic particulate material of from 80:20 to
20:80.
15. The process of any one of the preceding claims wherein step d) is carried out at a
temperature below 200 °C, preferably below 150 °C, more preferably below 100 °C.
16. The process of any one of the preceding claims whereby during step d) the biomass
material becomes coated onto the particulate inorganic material.
17. A composition consisting of solid biomass particles coated onto inorganic particulate
material
18. A composition consisting of lingo-cellulosic particles coated onto inorganic particulate
material
19. The process of any one of the preceding claims comprising the additional step of:
e) subjecting the mixture obtained in step d) to a fluid cracking process at a temperature
above 200 °C.
20. The process of claim 11 wherein step e) is carried out at a temperature in the range
of from 200 to 450 °C.
21. The process of claim 11 wherein step e) is carried out at a temperature in the range
of from 200 to 400 °C.
22. The process of any one of claims 1 through 16 comprising the additional step of:
e) subjecting the mixture obtained in step d) to a hydro treatment and/or conversion
process at a temperature above 200 °C.
23. The process of any one of claims 1 through 16 comprising the additional step of:
e) subjecting the mixture obtained in step d) to a hydrothermal conversion process
at a temperature above 100 °C.
24. The process of claim 23 wherein the hydrothermal conversion process is carried out
at a temperature above 200 °C.
25. The process of any of the preceding claims whereby step d) is performed in a fast
fluidized bed at catalyst flow velocities of at least 0.5 meters/second, preferably
1 m/sec
26. Process of any of the preceding claims whereby step d) is performed in a catalyst
riser or downer at catalyst flow velocities of at least 2 meters/second, preferably
higher than 10 m/sec
27. Process of any of the above claims whereby step b) is performed by milling the biomass
in a fluidized or moving bed with inorganic material.
28. Process of any of the above claims whereby in step b) a fluidizable biomass is produced.